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HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice
Adult neurogenesis, a striking form of neural plasticity, is involved in the modulation of social stimuli driving reproduction. Previous studies on adult neurogenesis have shown that this process is significantly modulated around puberty in female mice. Puberty is a critical developmental period tri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732626/ https://www.ncbi.nlm.nih.gov/pubmed/33328903 http://dx.doi.org/10.3389/fnana.2020.584493 |
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author | Trova, Sara Bovetti, Serena Pellegrino, Giuliana Bonzano, Sara Giacobini, Paolo Peretto, Paolo |
author_facet | Trova, Sara Bovetti, Serena Pellegrino, Giuliana Bonzano, Sara Giacobini, Paolo Peretto, Paolo |
author_sort | Trova, Sara |
collection | PubMed |
description | Adult neurogenesis, a striking form of neural plasticity, is involved in the modulation of social stimuli driving reproduction. Previous studies on adult neurogenesis have shown that this process is significantly modulated around puberty in female mice. Puberty is a critical developmental period triggered by increased secretion of the gonadotropin releasing hormone (GnRH), which controls the activity of the hypothalamic-pituitary-gonadal axis (HPG). Secretion of HPG-axis factors at puberty participates to the refinement of neural circuits that govern reproduction. Here, by exploiting a transgenic GnRH deficient mouse model, that progressively loses GnRH expression during postnatal development (GnRH::Cre;Dicer(loxP/loxP) mice), we found that a postnatally-acquired dysfunction in the GnRH system affects adult neurogenesis selectively in the subventricular-zone neurogenic niche in a sexually dimorphic way. Moreover, by examining adult females ovariectomized before the onset of puberty, we provide important evidence that, among the HPG-axis secreting factors, the circulating levels of gonadal hormones during pre-/peri-pubertal life contribute to set-up the proper adult subventricular zone-olfactory bulb neurogenic system. |
format | Online Article Text |
id | pubmed-7732626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77326262020-12-15 HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice Trova, Sara Bovetti, Serena Pellegrino, Giuliana Bonzano, Sara Giacobini, Paolo Peretto, Paolo Front Neuroanat Neuroscience Adult neurogenesis, a striking form of neural plasticity, is involved in the modulation of social stimuli driving reproduction. Previous studies on adult neurogenesis have shown that this process is significantly modulated around puberty in female mice. Puberty is a critical developmental period triggered by increased secretion of the gonadotropin releasing hormone (GnRH), which controls the activity of the hypothalamic-pituitary-gonadal axis (HPG). Secretion of HPG-axis factors at puberty participates to the refinement of neural circuits that govern reproduction. Here, by exploiting a transgenic GnRH deficient mouse model, that progressively loses GnRH expression during postnatal development (GnRH::Cre;Dicer(loxP/loxP) mice), we found that a postnatally-acquired dysfunction in the GnRH system affects adult neurogenesis selectively in the subventricular-zone neurogenic niche in a sexually dimorphic way. Moreover, by examining adult females ovariectomized before the onset of puberty, we provide important evidence that, among the HPG-axis secreting factors, the circulating levels of gonadal hormones during pre-/peri-pubertal life contribute to set-up the proper adult subventricular zone-olfactory bulb neurogenic system. Frontiers Media S.A. 2020-11-27 /pmc/articles/PMC7732626/ /pubmed/33328903 http://dx.doi.org/10.3389/fnana.2020.584493 Text en Copyright © 2020 Trova, Bovetti, Pellegrino, Bonzano, Giacobini and Peretto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Trova, Sara Bovetti, Serena Pellegrino, Giuliana Bonzano, Sara Giacobini, Paolo Peretto, Paolo HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title | HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title_full | HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title_fullStr | HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title_full_unstemmed | HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title_short | HPG-Dependent Peri-Pubertal Regulation of Adult Neurogenesis in Mice |
title_sort | hpg-dependent peri-pubertal regulation of adult neurogenesis in mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732626/ https://www.ncbi.nlm.nih.gov/pubmed/33328903 http://dx.doi.org/10.3389/fnana.2020.584493 |
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